Search Results (35)

This work focuses on the stability analysis of water-in-oil macroemulsions with a crude oil from the Sacha Field in Ecuador. This field is an important hydrocarbon resource in Ecuador with a typical bottom freshwater drive. The comprehensive stability analysis includes coalescence, water resolution or phase separation, and water–oil interfacial tension and interfacial dilatational viscoelastic modulus measurements over time. Two main parameters, due to their relevance, were controlled in these experiments: water salinity and temperature. The analysis reported here is the first focused on this important resource in Ecuador. Findings shed light on which mechanisms more likely control the stability of these water-in-oil macroemulsions. Results herein suggest that regardless of temperature, low-salinity water favors emulsion stability, likely due to the tendency of a stiffer interface formation at low-ionic strength, as interfacial viscoelasticity measurements show. This implies that the low-ionic strength water from the aquifer can enable the formation of stable emulsions. In contrast, water resolution depends significantly on temperature, possibly due to higher sedimentation rates. The implication is that if emulsions do not break up before cooling off, the emulsion can become more stable. Finally, analysis of the interface buildup rates could explain the observed increase in emulsion stability over time. Full article

The efficient separation of light hydrocarbons, particularly alkanes from their isomers (C₅–C₆), represents a significant and energy-intensive challenge for the petrochemical industry. Metal-Organic Frameworks (MOFs) offer promising solutions due to their exceptional porosity, surface area, and, crucially, their structural and chemical tunability. This study employs advanced computational methods, including Grand Canonical Monte Carlo (GCMC) simulations and Molecular Dynamics (MD), to systematically investigate the adsorption and separation of pentane isomers (n-pentane, isopentane, and neopentane) in the UiO-66 MOF family. Specifically, the impact of organic linker functionalization with -H (parent), -NH₂, -CH₃, and -COOH groups on adsorption isotherms, isosteric heats, and competitive behavior in mixtures is evaluated. The analysis provides a molecular-level view of host-guest and guest-guest interactions, elucidating the recognition and selectivity mechanisms governing the separation of these C5 isomers and the potential for engineering MOF materials for this application. Full article

A major problem in natural gas production is the waterlogging of gas wells. This problem occurs at the end of a well’s life when the reservoir pressure becomes low and the gas velocity in the well tubing is no longer sufficient to bring the gas-related fluids (water and gas condensate) up to the surface. This causes water to accumulate at the bottom of the gas well, which can seriously reduce or even stop gas production altogether. This paper presents a study of the foaming of reservoir water using foaming sticks with the trade names BioLight 30/380, BioCond 30, BioFoam 30, BioAcid 30/380, and BioCond Plus 30/380. The reservoir waters tested came from near-well separators located at three selected wells that had undergone waterlogging and experienced a decline in natural gas production. They were characterised by varying physical and chemical parameters, especially in terms of mineralisation and oil contaminant content. Laboratory studies on the effect of foaming agents on the effectiveness of foaming and lifting of reservoir water from the well were carried out on a laboratory bench, simulating a natural gas-producing column using surfactant doses in the range of 1.5–5.0 g/m³ and measuring the surface tension of the water, the volume of foam generated as a function of time and the foamed reservoir water. The performance criterion for the choice of surfactant for the test water was its effective lifting in a foam structure from an installation, simulating a waterlogged gas well and minimising the dose of foaming agent introduced into the water. The results obtained from the laboratory tests allowed the selection of effective surfactants in the context of foaming and uplift of reservoir water from wells, where a decline in natural gas production was observed as a result of their waterlogging. In the next stage, well tests were carried out based on laboratory studies to verify their effectiveness under conditions typical for the production site. Tests carried out at natural gas wells showed that the removal of water from the bottom of the well resulted in an increase in natural gas production, ranging from 56.3% to 79.6%. In practice, linking the results of laboratory tests for the type and dosage of foaming agents to the properties of reservoir water and gas production parameters made it possible to identify the types of surfactants and their dosages that improve the production of a given type of natural gas reservoir in an effective manner, resulting in an increase in the degree of depletion of hydrocarbon deposits. Full article

Oily sludge (OS) has long been regarded as a hazardous waste, and improper disposal may lead to serious environmental concerns and human health risks. Despite various methods having been proposed and applied to the treatment of OS, the oil occurrence states and properties in sludge are rarely characterized, which may directly link to the selection and effectiveness of treatment methods. Here, confocal laser scanning microscopy (CLSM), X-ray diffraction (XRD), gas chromatography (GC), and four components (SARA) analysis were utilized to characterize the changes in the oil occurrence states and compositions in OS samples before and after high-speed stirring (HSS) treatment. Our results show a substantial reduction in the oil concentration of OS after HSS treatment (from 32.98% to 1.65%), while SARA analysis reveals a similar oil composition before and after treatment, suggesting the broad applicability of HSS in removing oil and its insignificant selectivity towards various hydrocarbon components. This is further supported by the total petroleum hydrocarbon (TPH) analysis results, which show that the separated oil phase has a hydrocarbon composition similar to that of the original OS sample. The CLSM and fluorescence analysis suggest a homogeneous distribution of oil in the sludge, with relatively light components more concentrated in the pore systems between coarse mineral particles, whereas relatively heavy components tend to coexist with clay minerals. After HSS cleaning, both light and heavy components are removed to varying degrees, but light components are preferentially removed while heavy components tend to be retained in the sludge due to adsorption by clay minerals. This is consistent with TPH analysis, where a significant decrease in n-alkanes with lower carbon numbers (n-C14 to n-C20) was observed in the residual sample. Our findings demonstrate the dynamic response of oil occurrence states and compositions to the OS treatment process and highlight the importance of characterizing these fundamental properties prior to the selection of OS treatment methods. Full article

Plastics, once regarded as a revolutionary material shaping modern society, now pose an unprecedented threat to our environment. Household solid waste sorting stations produce several fractions, one of which contains a high concentration of Low-Density Polyethylene (LDPE) film waste (packaging, sunscreen film, etc.). This fraction is difficult to recycle because it contains quite a lot of impurities. Usually, it is sent to cement factories that burn it together with other fuels. However, with some processing techniques such as catalytic pyrolysis, this fraction could be valorized. In this paper, experiments were carried out in batches at a laboratory-scale installation, with a processing capacity of 1–3 kg of waste. A pyrolysis reactor was connected to a distillation column, enabling separation of the fractions. The gaseous and liquid fractions were characterized by GC-FID-TCD (gases) and GC-MS (liquids) analysis. Natural catalysts such as bentonite or clinoptilolite were studied and used in the melting of plastic mass to simplify the process as much as possible. To test the activity of the catalysts, the pyrolysis of LDPE granules was initially studied. It was found that natural zeolites are much more active than bentonite and that a minimum concentration of 5–10% is needed to have a positive effect on the composition of the fractions (increasing the weight of the light fractions (C1–C6, C6–C10, and C11–C13) in relation to the heavy fractions (C13–C20 and C20+). Catalytic pyrolysis gives a completely different distribution of light hydrocarbons. The best catalyst selected from LDPE lab experiments was then tested upon the pyrolysis of plastic film waste obtained by a waste treatment plant. The research objective reported in this paper was to obtain a fraction of combustible gases in the largest possible proportion, which can be much more easily exploited by burning in an engine that drives an electric generator. Full article

The exploration of continental shale oil in China has made a breakthrough in many basins, but the pure shale type has only been found in the Qingshankou Formation, Gulong Sag, Songliao Basin, and the evaluation of shale oil occurrence and sweet spot faces great challenges. Using information about the total organic carbon (TOC), Rock-Eval pyrolysis, vitrinite reflectance (Ro), kerogen elemental composition, carbon isotopes, gas chromatography (GC), bitumen extraction, and component separation, this paper systematically studies the organic geochemical characteristics and shale oil occurrence at the Qingshankou Formation. The G1 well, which was cored through the entire section of the Qingshankou Formation in the Gulong Sag, was the object of this study. On this basis, the favorable sweet spots for shale oil exploration are predicted. It is concluded that the shale of the Qingshankou Formation has high organic heterogeneity in terms of organic matter features. The TOC content of the source rocks in the Qingshankou Formation is enhanced with the increase in the burial depth, and the corresponding organic matter types gradually changed from Ⅱ₂ and Ⅱ₁ types to the Ⅰ type. The distribution of Ro ranges from 1.09% to 1.67%, and it is the mature to high-mature evolution stage that generates a large amount of normal crude oil and gas condensate. The high-quality source rocks of good to excellent grade are mainly distributed in the Qing 1 member and the lower part of the Qing 2 member. After the recovery of light hydrocarbons and the correction of pyrolytic heavy soluble hydrocarbons, it is concluded that the occurrence state of shale oil in the Qingshankou Formation is mainly the free-state form, with an average value of 6.9 mg/g, and there is four times as much free oil as adsorbed oil. The oil saturation index (OSI), mobile hydrocarbon content, Ro, and TOC were selected to establish the geochemical evaluation criteria for shale oil sweet spots in the Qingshankou Formation. The evaluation results show that interval 3 and interval 5 of the Qingshankou Formation in the G1 well are the most favorable sections for shale oil exploration. Full article

The photocatalytic reduction of CO₂ into hydrocarbons is a promising solution for the energy crisis and greenhouse gas emissions. Thus, the fabrication and development of a new type of photocatalyst is of great importance for the practical application of CO₂ reduction. Herein, we report a facile synthesis of Zn₂SnO₄ (ZTO) microspheres doped with Co³⁺ ions or Ni³⁺ ions. The doped Co³⁺/Ni³⁺ ions substitute the lattice Zn/Sn ions. DFT calculations and experimental results reveal that the doped Co³⁺/Ni³⁺ ions would induce new doping energy levels in the band gap, extend the light response from the UV to the visible region, and separate the charge carriers. As a result, compared with pure ZTO, the photocatalytic activity of a CO₂ reduction into CH₄ is significantly improved for Co-doped ZTO (Co-ZTO) and Ni-doped ZTO (Ni-ZTO). Full article

Soft tissue adhesion and sealing around dental and maxillofacial implants, related prosthetic components, and crowns are a clinical imperative to prevent adverse outcomes of periodontitis and periimplantitis. Zirconia is often used to fabricate implant components and crowns. Here, we hypothesized that UV treatment of zirconia would induce unique behaviors in fibroblasts that favor the establishment of a soft tissue seal. Human oral fibroblasts were cultured on zirconia specimens to confluency before placing a second zirconia specimen (either untreated or treated with one minute of 172 nm vacuum UV (VUV) light) next to the first specimen separated by a gap of 150 µm. After seven days of culture, fibroblasts only transmigrated onto VUV-treated zirconia, forming a 2.36 mm volume zone and 5.30 mm leading edge. Cells migrating on VUV-treated zirconia were enlarged, with robust formation of multidirectional cytoplastic projections, even on day seven. Fibroblasts were also cultured on horizontally placed and 45° and 60° tilted zirconia specimens, with the latter configurations compromising initial attachment and proliferation. However, VUV treatment of zirconia mitigated the negative impact of tilting, with higher tilt angles increasing the difference in cellular behavior between control and VUV-treated specimens. Fibroblast size, perimeter, and diameter on day seven were greater than on day one exclusively on VUV-treated zirconia. VUV treatment reduced surface elemental carbon and induced superhydrophilicity, confirming the removal of the hydrocarbon pellicle. Similar effects of VUV treatment were observed on glazed zirconia specimens with silica surfaces. One-minute VUV photofunctionalization of zirconia and silica therefore promotes human oral fibroblast attachment and proliferation, especially under challenging culture conditions, and induces specimen-to-specimen transmigration and sustainable photofunctionalization for at least seven days. Full article

Carbon hydrocarbon compounds, especially low-carbon hydrocarbons (C₁–C₃), are vital raw materials in the petrochemical industry, but their efficient separation has great challenges due to their similar molecular structures and properties. In contrast to traditional low-temperature distillation and absorption separation technologies, selective adsorption employing porous materials as adsorbent has the advantages of low energy consumption, high efficiency, and high selectivity, indicating broad application possibilities in the field of low-carbon hydrocarbon separation. In this paper, the recent progress in the separation and purification of hydrocarbon mixtures by means of the two kinds of porous materials (metal–organic frameworks and molecular sieves) that have been widely used in recent years is reviewed, including purification of methane and separation of ethylene/ethane, propylene/propane, and some high-carbon hydrocarbon isomers. The structure–activity relationships between their chemical composition, structural characteristics, and separation performance are discussed to understand the separation mechanism. In conclusion, the issues encountered in the application of metal–organic frameworks and molecular sieves in the separation of low-carbon hydrocarbons are discussed in light of the current context of “carbon neutrality”. Full article

Easily soluble organic components in Santanghu long flame coal (SLFC) from Hami (Xinjiang, China) were separated by CS₂ and acetone mixed solvent (v/v = 1:1) under ultrasonic condition, and the extract residue was stratified by carbon tetrachloride to obtain the light raffinate component (SLFC-L). The effect of solvent treatment on the composition and structure of the coal and its rapid pyrolysis products was analyzed. Solvent treatment can reduce the moisture content in coal from 9.48% to 6.45% and increase the volatile matter from 26.59% to 28.78%, while the macromolecular structure of the coal changed slightly, demonstrating the stability of coal’s complex organic structure. Compared with raw coal, the relative contents of oxygen-containing functional groups and aromatic groups in SLFC-L are higher, and the weight loss rates of both SLFC and SLFC-L reached the maximum at about 450 °C. In contrast, the loss rate of SLFC-L is more obvious, being 33.62% higher than that of SLFC. Pyrolysis products from SLFC at 450 °C by Py-GC/MS are mainly aliphatic hydrocarbons and oxygenated compounds, and the relative contents of aliphatic hydrocarbons decreased from 48.48% to 36.13%, while the contents of oxygenates increased from 39.07% to 44.95%. Overall, the composition and functional group in the coal sample were changed after solvent treatment, resulting in a difference in the composition and distribution of its pyrolysis products. Full article

The separation of light hydrocarbon compounds is an important process in the chemical industry. Currently, its separation methods mainly include distillation, membrane separation, and physical adsorption. However, these traditional methods or materials have some drawbacks and disadvantages, such as expensive equipment costs and high energy consumption, poor selectivity, low separation ratios, and separation efficiencies. Therefore, it is important to develop novel separation materials for light hydrocarbon separation. As a new type of organic–inorganic hybrid crystalline material, metal–organic frameworks (MOFs) are promising materials for light hydrocarbon separation due to their designability of structure and easy modulation of function. This review provides an overview of recent advances in the design, synthesis, and application of MOFs for light hydrocarbon separation in recent years, with a focus on the separation of alkane, alkene, and alkyne. We discuss strategies for improving the adsorption selectivity and capacity of MOFs, including pore size limitation, physical adsorption, and chemisorption. In addition, we discuss the advantages/disadvantages, challenges, and prospects of MOFs in the separation of light hydrocarbon. Full article

Stabilization of condensate is a highly energy-consuming process compared to other oil and gas processes. There is a need to reduce this energy consumption. Therefore, the present work aims to simulate the stabilization unit in terms of available energy and on-spec stabilized condensate products. Natural gas condensate liquids (NGL) need to be stabilized by eliminating lighter hydrocarbon gases and acid gases before being sent to the refinery. Stabilized NGL has the vapor pressure determined as a Reid vapor pressure of 7 psia, showing that light components did not evolve as a separate gas phase. Stabilization and CO₂ removal was performed through the distillation method by heating and pressure reduction using steady state and dynamic simulation through Aspen HYSYS. Different process alterations around the exchanger and column have been studied based on the utilities available for the stabilization and CO₂ removal process. Sensitivity studies, including the impact of CO₂ concentration, the temperature at the inlet of the stabilizer flash separator, and the dynamic simulation for the PID controller, have been performed to analyze the impact on the process parameters, such as Reid vapor pressure (RVP) and CO₂ of the rundown air cooler and heat duties of the exchangers. Actual plant data have been used for the validation of process simulation values for the accuracy of the condensate stabilization unit model. Based on the scenarios analyzed, it can be concluded that the nitrogen stripping method achieved 7 ppmv CO₂ and 7 psia RVP in the condensate from the cooler outlet, while a variation of 29 bpd was observed for the stabilized condensate flowrate throughout all scenarios with data validation showing 0.24% discrepancy between Aspen Hysys data and actual plant data. Full article

Separating light hydrocarbons (C₂H₆, C₃H₈, and C₄H₁₀) from CH₄ is challenging but important for natural gas upgrading. A microporous metal-organic framework, Zn(bdc)(ted)_0.5, based on terephthalic acid (bdc) and 1,4-diazabicyclo[2.2.2]octane (ted) ligands, is synthesized and characterized through various techniques, including powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and porosity analysis. The adsorption isotherms of light hydrocarbons on the material are measured and the isosteric adsorption heats of CH₄, C₂H₆, C₃H₈, and C₄H₁₀ are calculated. The prediction of C2–4/C1 adsorption selectivities is accomplished using ideal adsorbed solution theory (IAST). The results indicate that the material exhibits exceptional characteristics, including a Brunauer-Emmett-Teller (BET) surface area of 1904 m²/g and a pore volume of 0.73 cm³/g. Notably, the material demonstrates remarkable C₂H₆ adsorption capacities (4.9 mmol/g), while CH₄ uptake remains minimal at 0.4 mmol/g at 298 K and 100 kPa. These findings surpass those of most reported MOFs, highlighting the material’s outstanding performance. The isosteric adsorption heats of C₂H₆, C₃H₈, and C₄H₁₀ on the Zn(bdc)(ted)_0.5 are higher than CH₄, suggesting a stronger interaction between C₂H₆, C₃H₈, and C₄H₁₀ molecules and Zn(bdc)(ted)_0.5. The molecular simulation reveals that Zn(bdc)(ted)_0.5 prefers to adsorb hydrocarbon molecules with richer C-H bonds and larger polarizability, which results in a stronger dispersion force generated by an adsorbent-adsorbate induced polarization effect. Therefore, the selectivity of C₄H₁₀/CH₄ is up to 180 at 100 kPa, C₃H₈/CH₄ selectivity is 67, and the selectivity of C₂H₆/CH₄ is 13, showing a great potential for separating C2–4 over methane. Full article

Yinggema lignite (YL) was pretreated with isometric acetone/carbon disulfide mixed solvent to obtain the residue (R_YL) and, then, R_YL was separated by density difference with carbon tetrachloride to obtain the light residue (LR_YL). The flash pyrolysis performances of YL and LR_YL were analyzed by thermogravimetry–Fourier transform infrared spectrometer–Gas chromatography/mass spectrometer (TG-FTIR-GC/MS). The results showed that solvent pretreatment could remove some small molecules in the coal and swell the used coal, leading to the increase in pyrolysis reactivity. The intensity and absorption peak area of C=O from LR_YL were significantly reduced compared to YL, resulting from the high hydrogen-donating ability of acetone. The main gaseous products of both samples are H₂O, CH₄, CO₂, and CO; the hydrocarbons detected by GC/MS in the pyrolysis products of YL and LR_YL at 450 °C were mainly alkanes, alkenes, and arenes, with the higher relative contents of alkanes of 31.1% and 36.2%, followed by arenes of 27.1% and 22.6%, respectively. The oxygen-containing compounds were mainly alcohols and phenols. It is speculated that the pretreated coal could expose more oxygen-containing functional groups, facilitating their conversion to phenolic hydroxyl groups during the pyrolysis process, resulting in more phenolic compounds. Full article

Photocatalytic CO₂ reduction into hydrocarbon fuels is one of the most efficient processes since it serves as a renewable energy source while also lowering atmospheric CO₂ levels. The development of appropriate materials and technology to attain greater yield in CO₂ photoreduction is one of the key issues facing the 21st century. This study successfully fabricated novel ternary reduced graphene oxide (RGO)/Au-TiO₂ nanotube arrays (TNTAs) photocatalysts to promote CO₂ photoreduction to CH₄. Visible light-responsive RGO/Au-TNTAs composite was synthesized by facile electrochemical deposition of Au nanoparticles (NPs) and immersion of RGO nanosheets onto TNTAs. The synthesized composite has been thoroughly investigated by FESEM, HR-TEM, XRD, XPS, FT-IR, UV-Vis DRS, and PL analyzer to explain structural and functional performance. Under the source of visible light, the maximum yield of CH₄ was attained at 35.13 ppm/cm² for the RGO/Au-TNTAs composite photocatalyst after 4 h, which was considerably higher by a wide margin than that of pure TNTAs, Au-TNTAs and RGO-TNTAs. The CO₂ photoreduction of the RGO/Au-TNTAs composite has been improved due to the combined effects of Au NPs and RGO. Due to its surface plasmonic resonance (SPR) mechanism, Au NPs play a crucial role in the absorption of visible light. Additionally, the middle RGO layers serve as effective electron transporters, facilitating better separation of electron-hole pairs. The newly constructed composite would be a promising photocatalyst for future photocatalytic applications in other fields. Full article